DNA and Chromatin Imaging with Super-Resolution Fluorescence Microscopy Based on Single-Molecule Localization

被引:51
|
作者
Flors, Cristina [1 ,2 ]
机构
[1] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
[2] Univ Edinburgh, COSMIC, Edinburgh EH9 3JJ, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
super-resolution fluorescence microscopy; DNA intercalators; photophysics; single-molecule methods; CYANINE DYES; BIS-INTERCALATION; DIFFRACTION-LIMIT; RESOLUTION; BINDING; PROBES; YOYO; NANOSCOPY; KINETICS; CELLS;
D O I
10.1002/bip.21574
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
With the expansion of super-resolution fluorescence microscopy methods, it is now possible to access the organization of cells and materials at the nanoscale by optical means. This review discusses recent progress in super-resolution imaging of isolated and cell DNA using single-molecule localization methods. A high labeling density of photoswitchable fluorophores is crucial for these techniques, which can be provided by sequence independent DNA stains in which photoblinking reactions can be induced. In particular, unsymmetrical cyanine intercalating dyes in combination with special buffers can be used to image isolated DNA with a spatial resolution of 30-40 nm. For super-resolution imaging of chromatin, cell permeant cyanine dyes that bind the minor groove of DNA have the potential to become a useful alternative to the labeling of histones and other DNA-associated proteins. Other recent developments that are interesting in this context such as high density labeling methods or new DNA probes with photoswitching functionalities are also surveyed. Progress in labeling, optics, and single-molecule localization algorithms is being rapid, and it is likely to provide real insight into DNA structuring in cells and materials. (C) 2010 Wiley Periodicals, Inc. Biopolymers 95: 290-297, 2011.
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页码:290 / 297
页数:8
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